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表皮生长因子、转化生长因子α和神经生长因子对大鼠胃黏膜完整性和微循环的影响

Effect of epidermal growth factor, transforming growth factor alpha and nerve growth factor on gastric mucosal integrity and microcirculation in the rat.

作者信息

Tepperman B L, Soper B D

机构信息

Department of Physiology, Faculty of Medicine, University of Western Ontario, London, Canada.

出版信息

Regul Pept. 1994 Feb 3;50(1):13-21. doi: 10.1016/0167-0115(94)90186-4.

Abstract

In the present study we have compared the effects of the peptide growth factors epidermal growth factor (EGF), transforming growth factor alpha (TGF alpha) and nerve growth factor (NGF) on gastric mucosal integrity and mucosal blood flow in the rat. Mucosal damage was assessed 30 min after intraluminal instillation of 40% (w/v) ethanol (EtOH). EtOH treatment resulted in an increase in mucosal damage when compared to saline treated control animals. Administration of each growth factor either by tail vein (i.v.; 0.2-1 nmol/kg) or via the left gastric artery (i.a.; 0.05-0.2 nmol/kg) resulted in a significant reduction in the extent of mucosal damage. The growth factors reduced EtOH-mediated damage in an equipotent manner. The reduction in the area hemorrhagic damage ranged from -25 to -35% from EtOH alone when the factors were administered i.a. and from -75 to -85% when delivered i.v. Gastric mucosal blood flow as assessed by laser Doppler flowmetry (LDF) was increased in a dose-dependent and equipotent manner by EGF and TGF alpha administered either by the i.v. or i.a. route. LDF changes were greater when EGF or TGF alpha were delivered via the i.a. route. NGF did not significantly increase blood flow regardless of the dose or route of delivery. beta-Adrenoceptor blockade with propranolol (0.75 mg/kg i.v.) abolished the increase in LDF in response to EGF or TGF alpha but did not affect the ability of these growth factors to reduce EtOH-mediated damage.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在本研究中,我们比较了肽生长因子表皮生长因子(EGF)、转化生长因子α(TGFα)和神经生长因子(NGF)对大鼠胃黏膜完整性和黏膜血流量的影响。在向管腔内注入40%(w/v)乙醇(EtOH)30分钟后评估黏膜损伤情况。与用生理盐水处理的对照动物相比,EtOH处理导致黏膜损伤增加。通过尾静脉(静脉注射;0.2 - 1 nmol/kg)或经胃左动脉(动脉内注射;0.05 - 0.2 nmol/kg)给予每种生长因子,均导致黏膜损伤程度显著降低。这些生长因子以等效方式减少了EtOH介导的损伤。当通过动脉内注射给予这些因子时,出血性损伤面积的减少幅度为单独使用EtOH时的 - 25%至 - 35%,静脉注射时为 - 75%至 - 85%。通过激光多普勒血流仪(LDF)评估,静脉注射或动脉内注射给予的EGF和TGFα以剂量依赖性和等效方式增加了胃黏膜血流量。当EGF或TGFα通过动脉内注射途径给药时,LDF变化更大。无论给药剂量或途径如何,NGF均未显著增加血流量。用普萘洛尔(0.75 mg/kg静脉注射)进行β - 肾上腺素能受体阻断消除了对EGF或TGFα反应时LDF的增加,但不影响这些生长因子减少EtOH介导损伤的能力。(摘要截短于250字)

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